{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Dover",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94926",
      "recalling_firm": "LINK BIO CORP",
      "address_1": "69 King St Ste 2",
      "address_2": "",
      "postal_code": "07801-2800",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of FL, GA, KS, OH, WI.",
      "recall_number": "Z-2445-2024",
      "product_description": "LINK SymphoKnee Patella Sizing Template, Item Number 881-509/00",
      "product_quantity": "8 units",
      "reason_for_recall": "The LinkSymphoKnee Patella Sizing Template was incorrectly labeled. The markings on two arms of the instrument were mixed up because the triangular Patella Sizing Template was inserted upside down into the laser marking process.",
      "recall_initiation_date": "20240627",
      "center_classification_date": "20240725",
      "report_date": "20240731",
      "code_info": "Item Number: 881-509/00; UDI-DI: 04026575310203; Lot number: C225066.",
      "more_code_info": ""
    }
  ]
}